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FDA 510(k)

KIMLON UNIVERSAL DRAPE

K-Number: K790636 · 1979-05-08

ApplicantKimberly-Clark Corp.
Decision Date1979-05-08
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KIMLON UNIVERSAL DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark Corp.. It received FDA 510(k) clearance on 1979-05-08 under 510(k) number K790636. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIMLON UNIVERSAL DRAPE?

KIMLON UNIVERSAL DRAPE is a medical device that received FDA 510(k) clearance on 1979-05-08. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K790636.

When did KIMLON UNIVERSAL DRAPE receive FDA 510(k) clearance?

KIMLON UNIVERSAL DRAPE received FDA 510(k) clearance on 1979-05-08, under 510(k) number K790636.

Who is the listed applicant for KIMLON UNIVERSAL DRAPE?

The FDA 510(k) record lists Kimberly-Clark Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIMLON UNIVERSAL DRAPE?

The FDA product code for KIMLON UNIVERSAL DRAPE is KKX.

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Other records listing Kimberly-Clark Corp. as applicant

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Related Devices (Code: KKX)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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